Dyschromatosis universalis hereditaria

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A rare genetic pigmentation anomaly of the skin characterized by generalized irregularly shaped asymptomatic hyper- and hypopigmented macules distributed in a reticular pattern involving the trunk limbs and sometimes the face. The palms soles and mucosa are usually not affected. Systemic abnormalities have been rarely reported.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version July 2024

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Dyschromatosis universalis hereditaria?

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